FDA inspection
audifon GmbH & Co. KG: FDA inspection ending May 11, 2017
FDA inspection 1013135 · Voluntary Action Indicated (VAI) · Kolleda
Key facts
| Inspection ID | 1013135 |
|---|---|
| Firm | audifon GmbH & Co. KG |
| FEI number | 3006076696 |
| Address | Werner-von-Siemens-Str. 2 |
| City | Kolleda |
| Country | Germany |
| Fiscal year | 2017 |
| Inspection end date | May 11, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data